Sahoo Nibedita, Mishra Pritinanda, Patra Susama, Sasmal Prakash Kumar
Senior Resident, Department of Pathology, AIIMS, Bhubaneswar, Odisha, India.
Associate Professor, Department of Pathology, AIIMS, Bhubaneswar, Odisha, India.
J Clin Diagn Res. 2017 Jun;11(6):ED16-ED17. doi: 10.7860/JCDR/2017/27937.10098. Epub 2017 Jun 1.
Handful cases of invasive Cystic Hypersecretory Ductal Carcinoma (CHC) have been reported so far in literature. Cystic hypersecretory lesions of breast have a spectrum of morphological features ranging from Cystic Hypersecretory Hyperplasia (CHH), CHH with atypia, in situ to invasive CHC. We are reporting a case of a 32-year-old female who had nipple discharge and lump in her right breast for one month. A modified radical mastectomy was done and morphological diagnosis of invasive CHC with axillary node metastasis was made. The postoperative events were uneventful. Invasive CHC being a rare entity, our understanding of its biological behavior, prognostic factors and genetic basis is limited. The authors are aware of only 15 similar cases being reported in the English literature.
迄今为止,文献中仅报道了少数几例浸润性囊性高分泌导管癌(CHC)。乳腺的囊性高分泌性病变具有一系列形态学特征,从囊性高分泌性增生(CHH)、非典型性CHH、原位癌到浸润性CHC。我们报告了一例32岁女性,其右乳出现乳头溢液和肿块1个月。行改良根治性乳房切除术,形态学诊断为浸润性CHC伴腋窝淋巴结转移。术后情况平稳。浸润性CHC是一种罕见的实体,我们对其生物学行为、预后因素和遗传基础的了解有限。作者仅知晓英文文献中报道了15例类似病例。